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Updated: Jun 20, 2026

Determination of Inorganic Arsenic in a Wide Range of Food Matrices using Hydride Generation - Atomic Absorption Spectrometry.
Published on: September 1, 2017
Discrimination of thioarsenites and thioarsenates by X-ray absorption spectroscopy
Elke Suess1, Andreas C Scheinost, Benjamin C Bostick
1Environmental Geochemistry, University of Bayreuth, Universitaetsstrasse 30, 95440 Bayreuth, Germany. elke.suess@uni-bayreuth.de
Abstract:
Soluble arsenic-sulfur compounds play important roles in the biogeochemistry of arsenic in sulfidic waters but conflicting analytical evidence identifies them as either thioarsenates (= As(V)-sulfur species) or thioarsenites (= As(III)-sulfur species). Here, we present the first characterization of thioarsenates (mono-, di-, and tetrathioarsenate) by X-ray absorption spectroscopy and demonstrate that their spectra are distinctly different from those of As(III)-sulfur species, as well as from arsenite and arsenate. The absorption near edge energy decreases in the order arsenate > thioarsenates > arsenite > As(III)-sulfur species, and individual thioarsenates differ by 1 eV per sulfur atom. Fitted As(V)-S and As(V)-O bond distances in thioarsenates (2.13-2.18 A and 1.70 A, respectively) are significantly shorter than the corresponding As(III)-S and As(III)-O bond distances in As(III)-S species (2.24-2.34 A and 1.78 A, respectively). Finally, we demonstrate that thioarsenates can be identified by principal component analysis in mixtures containing As(III)-sulfur species. This capability is used to study the spontaneous reduction of tetrathioarsenate to As(III)-sulfur species (possibly trithioarsenite) upon acidification from pH 9.5 to 2.8.
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